1. Badaruddoza, Shadab GG, Afzal M, Ahmad MD (2000) Genetic analysis of fragile X-syndrome.Indian J Med Sci. May; 54 (5): 174–6.
2. Ballo R, Viljoen D, Beighton P (1994) Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 person affected. S Afr Med J 84 (8 Pt 1): 494–7
3. Bamshad M, Kivisild T, Watkins WS, Dixon ME, Ricker CE, Rao BB, Naidu JM et al. (2001) Genetic evidence on the origins of Indian caste populations. Genome Res 11: 994–1004
4. Bannerjee M, Verma IC (1997) Are there ethnic differences in deletions in the dystrophin gene Am J Med Genet 68(2): 152–7.
5. Baskaran S, Naseerullah MK, Manjunatha KR, Chetan GK, Arthi R, Rao GV, Girimaji SR, Srinath S, Sheshadri S, Devi RR, Brahmachari V. (1998) Triplet repeat polymorphism and fragile X syndrome in the Indian context.Indian J Med Res. Jan; 107: 29–36